176 related articles for article (PubMed ID: 7681735)
1. Guadalajara camptodactyly syndrome type I. A corroborative family.
Figuera LE; Ramírez-Dueñas ML; García-Cruz D; Villar V; Cantú JM
Clin Genet; 1993 Jan; 43(1):11-5. PubMed ID: 7681735
[TBL] [Abstract][Full Text] [Related]
2. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
Cantú JM; Rivera H; Nazará Z; Rojas Q; Hernández A; García-Cruz D
Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
[TBL] [Abstract][Full Text] [Related]
3. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance.
Pena SD; Shokeir MH
Birth Defects Orig Artic Ser; 1976; 12(5):201-8. PubMed ID: 953225
[No Abstract] [Full Text] [Related]
4. A new syndrome with camptodactyly, joint contractures, facial anomalies, and skeletal defects: a case report and review of syndromes with camptodactyly.
Rozin MM; Hertz M; Goodman RM
Clin Genet; 1984 Oct; 26(4):342-55. PubMed ID: 6437708
[TBL] [Abstract][Full Text] [Related]
5. Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndrome.
Goodman RM; Katznelson MB; Hertz M; Katznelson A
J Med Genet; 1976 Apr; 13(2):136-41. PubMed ID: 933111
[TBL] [Abstract][Full Text] [Related]
6. Hyperphosphatasia with mental retardation, brachytelephalangy, and a distinct facial gestalt: Delineation of a recognizable syndrome.
Horn D; Schottmann G; Meinecke P
Eur J Med Genet; 2010; 53(2):85-8. PubMed ID: 20080219
[TBL] [Abstract][Full Text] [Related]
7. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family.
Gollop TR; Colletto GM
Am J Med Genet; 1984 Feb; 17(2):399-406. PubMed ID: 6702893
[TBL] [Abstract][Full Text] [Related]
8. Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: autosomal recessive entity?
Kilic I; Kilic BA; Ergin H; Aygün MG; Aksit MA
Am J Med Genet; 1998 Apr; 77(1):28-30. PubMed ID: 9557890
[TBL] [Abstract][Full Text] [Related]
9. Guadalajara camptodactyly type III: a new probably autosomal dominant syndrome.
Figuera LE; Ramírez-Dueñas ML; Dávalos IP; Cantú JM
Clin Dysmorphol; 2002 Oct; 11(4):243-7. PubMed ID: 12401988
[TBL] [Abstract][Full Text] [Related]
10. Marden-Walker syndrome in two siblings.
Chia FL; Chia F
J Paediatr Child Health; 1993 Aug; 29(4):312-4. PubMed ID: 7690581
[TBL] [Abstract][Full Text] [Related]
11. Guadalajara camptodactyly syndrome type II.
Cantú JM; García-Cruz D; Gil-Viera J; Nazará Z; Ramírez ML; Solé-Pujol MT; Sánchez-Corona J
Clin Genet; 1985 Jul; 28(1):54-60. PubMed ID: 4040823
[TBL] [Abstract][Full Text] [Related]
12. Guadalajara camptodactyly syndrome type I: report on a new case.
Zechi-Ceide RM; Guion-Almeida ML; Richieri-Costa A
Clin Dysmorphol; 2002 Apr; 11(2):129-32. PubMed ID: 12002144
[TBL] [Abstract][Full Text] [Related]
13. [Differential diagnostic considerations in microcephalic dwarfism].
Kraft CN; Diedrich O; Wagner U; Schmitt O
Z Orthop Ihre Grenzgeb; 2000; 138(2):126-30. PubMed ID: 10820877
[TBL] [Abstract][Full Text] [Related]
14. Greig cephalopolysyndactyly: report of 13 affected individuals in three families.
Baraitser M; Winter RM; Brett EM
Clin Genet; 1983 Oct; 24(4):257-65. PubMed ID: 6641002
[TBL] [Abstract][Full Text] [Related]
15. Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes: a possible new autosomal recessive disorder.
Gül D; Oktenli C; Sağlam M; Erdem U
Clin Dysmorphol; 2000 Jan; 9(1):61-2. PubMed ID: 10649801
[TBL] [Abstract][Full Text] [Related]
16. Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.
Tylki-Szymanska A
Am J Med Genet; 1986 Mar; 23(3):759-63. PubMed ID: 3953674
[TBL] [Abstract][Full Text] [Related]
17. Parental consanguinity in two sibs with omodysplasia.
Baxová A; Maroteaux P; Barosová J; Netriová I
Am J Med Genet; 1994 Feb; 49(3):263-5. PubMed ID: 8209882
[TBL] [Abstract][Full Text] [Related]
18. Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome.
Roifman CM; Chitayat D
Clin Genet; 2009 Nov; 76(5):449-57. PubMed ID: 19863561
[TBL] [Abstract][Full Text] [Related]
19. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
Froster UG; Rehder H; Höhn W; Oberheuser F
Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
[TBL] [Abstract][Full Text] [Related]
20. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.
Clayton-Smith J; Donnai D
J Med Genet; 1989 May; 26(5):339-42. PubMed ID: 2732996
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]